A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv972939



Internal ID15920209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:127543914..127685006hg38UCSC Ensembl
Innerchr3:127262757..127403849hg19UCSC Ensembl
Innerchr3:128745447..128886539hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38141093
hg19141093
hg18141093
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591580
Supporting Variants
Samples
Known GenesABTB1, MCM2, MIR6825, PODXL2, TPRA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv972939
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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